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Circulating CTRP9 correlates with the prevention of aortic calcification in renal allograft recipients

PloS one, 2020-01, Vol.15 (1), p.e0226526-e0226526

2020

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High molecular weight adiponectin inhibits vascular calcification in renal allograft recipients

PloS one, 2018-05, Vol.13 (5), p.e0195066-e0195066

2018

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Early, Noninvasive Clinical Indicators of Kidney Prognosis in Primary Nephrotic Syndrome: A Retrospective Exploratory Study

International journal of nephrology, 2022-08, Vol.2022, p.1-7

2022

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Steroid-sensitive recurrent mesangial proliferative glomerulonephritis with monoclonal IgG deposits

CEN case reports, 2021-05, Vol.10 (2), p.308-313

2021

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Severe electrolytes disorders with the interstitial kidney alterations in the patient with the history of total thyroidectomy and parathyroidectomy: possible role of vitamin D deficiency

Clinical case reports, 2018-06, Vol.6 (6), p.983-989

2018

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Steroid-sensitive recurrent mesangial proliferative glomerulonephritis with monoclonal IgG deposits

CEN case reports, 2021, Vol.10 (2), p.308-313

2021

Volltextzugriff (PDF)

Severe electrolytes disorders with the interstitial kidney alterations in the patient with the history of total thyroidectomy and parathyroidectomy: possible role of vitamin D deficiency

Clinical case reports, 2018, Vol.6 (6), p.983-989

2018

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Maximum Power Point Tracking of Multiple Photovoltaic Arrays: A PSO Approach

IEEE transactions on aerospace and electronic systems, 2011-01, Vol.47 (1), p.367-380

2011

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Chronic pathophysiological changes in the normal brain parenchyma caused by radiotherapy accelerate glioma progression

Scientific reports, 2021-11, Vol.11 (1), p.22110-22110, Article 22110

2021

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Two families with TET3-related disorder showing neurodevelopmental delay with craniofacial dysmorphisms

Journal of human genetics, 2022-03, Vol.67 (3), p.157-164

2022

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Biallelic null variants in ZNF142 cause global developmental delay with familial epilepsy and dysmorphic features

Journal of human genetics, 2022-03, Vol.67 (3), p.169-173

2022

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Persistent elevation of lysophosphatidylcholine promotes radiation brain necrosis with microglial recruitment by P2RX4 activation

Scientific reports, 2022-05, Vol.12 (1), p.8718-8718, Article 8718

2022

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ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndrome

Journal of human genetics, 2017-08, Vol.62 (8), p.741-746

2017

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A novel homozygous CHMP1A variant arising from segmental uniparental disomy causes pontocerebellar hypoplasia type 8

Journal of human genetics, 2023-04, Vol.68 (4), p.247-253

2023

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Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

Nature genetics, 2012-04, Vol.44 (4), p.376-378

2012

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Distal arthrogryposis in a girl arising from a novel TNNI2 variant inherited from paternal somatic mosaicism

Journal of human genetics, 2023-05, Vol.68 (5), p.363-367

2023

Volltextzugriff (PDF)

Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy

Journal of human genetics, 2021-04, Vol.66 (4), p.401-407

2021

Volltextzugriff (PDF)

Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome

Human mutation, 2017-06, Vol.38 (6), p.637-648

2017

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Pathogenic 12-kb copy-neutral inversion in syndromic intellectual disability identified by high-fidelity long-read sequencing

Genomics (San Diego, Calif.), 2021-01, Vol.113 (1), p.1044-1053

2021

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Novel CLTC variants cause new brain and kidney phenotypes

Journal of human genetics, 2022-01, Vol.67 (1), p.1-7

2022

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FPFS Shear Estimator: Systematic Tests on the Hyper Suprime-Cam Survey First-year Data

The Astrophysical journal. Supplement series, 2020-12, Vol.251 (2), p.19

2020

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De novo SOX11 mutations cause Coffin-Siris syndrome

Nature communications, 2014-06, Vol.5 (1), p.4011-4011, Article 4011

2014

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Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disorders

Human molecular genetics, 2018-04, Vol.27 (8), p.1421-1433

2018

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Association between cerebrospinal fluid parameters and developmental and neurological status in glucose transporter 1 deficiency syndrome

Journal of the neurological sciences, 2023-04, Vol.447, p.120597-120597, Article 120597

2023

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Circulating CTRP9 correlates with the prevention of aortic calcification in renal allograft recipients

High molecular weight adiponectin inhibits vascular calcification in renal allograft recipients

Comparison of the pain-reducing effects of EMLA cream and of lidocaine tape during arteriovenous fistula puncture in patients undergoing hemodialysis: A multi-center, open-label, randomized crossover trial

Early, Noninvasive Clinical Indicators of Kidney Prognosis in Primary Nephrotic Syndrome: A Retrospective Exploratory Study

Steroid-sensitive recurrent mesangial proliferative glomerulonephritis with monoclonal IgG deposits

Severe electrolytes disorders with the interstitial kidney alterations in the patient with the history of total thyroidectomy and parathyroidectomy: possible role of vitamin D deficiency

Steroid-sensitive recurrent mesangial proliferative glomerulonephritis with monoclonal IgG deposits

Severe electrolytes disorders with the interstitial kidney alterations in the patient with the history of total thyroidectomy and parathyroidectomy: possible role of vitamin D deficiency

Maximum Power Point Tracking of Multiple Photovoltaic Arrays: A PSO Approach

Chronic pathophysiological changes in the normal brain parenchyma caused by radiotherapy accelerate glioma progression

Two families with TET3-related disorder showing neurodevelopmental delay with craniofacial dysmorphisms

Biallelic null variants in ZNF142 cause global developmental delay with familial epilepsy and dysmorphic features

Persistent elevation of lysophosphatidylcholine promotes radiation brain necrosis with microglial recruitment by P2RX4 activation

ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndrome

A novel homozygous CHMP1A variant arising from segmental uniparental disomy causes pontocerebellar hypoplasia type 8

Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

Distal arthrogryposis in a girl arising from a novel TNNI2 variant inherited from paternal somatic mosaicism

Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy

Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome

Pathogenic 12-kb copy-neutral inversion in syndromic intellectual disability identified by high-fidelity long-read sequencing

Novel CLTC variants cause new brain and kidney phenotypes

FPFS Shear Estimator: Systematic Tests on the Hyper Suprime-Cam Survey First-year Data

De novo SOX11 mutations cause Coffin-Siris syndrome

Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disorders

Association between cerebrospinal fluid parameters and developmental and neurological status in glucose transporter 1 deficiency syndrome

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